1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070472 | early-onset epilepsy 3 | An epilepsy characterized by infantile or childhood onset of various types of seizures with variable global developmental delay and intellectual disability that has_material_basis_in heterozygous mutation in the ATP6V0C gene on chromosome 16p13.3. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:936 | brain disease | A central nervous system disease that is located_in the brain. |